Department of Psychiatry and Psychotherapy, Klinikum rechts der Isar, Technische Universitat Munchen, Mohlstr. 26, 81675 Munchen, Germany.
Curr Alzheimer Res. 2013 Jan;10(1):82-5.
Mild cognitive impairment (MCI) is a syndrome heterogeneous with regards to etiology and prognosis. Amyloid imaging enables to visualize a hallmark pathology of Alzheimer's disease (AD). Therefore we aimed to assess the usefulness of [(11)C]PiB PET for predicting clinical outcome of MCI patients after an interval of 2 years.
In 28 MCI participants with a global CDR rating at baseline of 0.5 a baseline examination including clinical assessments and [(11)C]PiB PET imaging and a clinical follow-up examination after a planned interval of 24 months were performed. Predictive values and accuracy of amyloid-positive and negative scans for conversion to dementia of any type and to dementia due to AD were calculated and compared to neuropsychological tests and ApoE genotyping.
Of 17 MCI patients who were amyloid-positive at baseline converted 9 to dementia all of the AD type. 3 of the 11 amyloid-negative MCI subjects converted to dementia but none to dementia due to AD. PPV, NPV and accuracy (to dementia: 0.53, 0.73 and 0.61; to AD: 0.53, 1.00 and 0.70) was comparable to neuropsychological tests and superior to ApoE genotyping.
All MCI subjects who converted to dementia due to AD were amyloid-positive. However, only 50% of these MCI due to AD, intermediate likelihood, patients developed manifest dementia due to AD after 24 months limiting the usefulness of [(11)C]PiB PET for individual prediction of clinical outcome.
轻度认知障碍(MCI)是一种病因和预后均存在异质性的综合征。淀粉样蛋白成像能够使阿尔茨海默病(AD)的标志性病理可视化。因此,我们旨在评估[(11)C]PiB PET 在 2 年后对 MCI 患者临床结局的预测价值。
在 28 名基线时全球临床痴呆评定量表(CDR)评分为 0.5 的 MCI 参与者中,进行基线检查,包括临床评估和[(11)C]PiB PET 成像,以及在计划的 24 个月间隔后进行临床随访检查。计算并比较淀粉样蛋白阳性和阴性扫描对任何类型痴呆和 AD 所致痴呆的转化率的预测值和准确率,以及与神经心理学测试和 ApoE 基因分型的相关性。
17 名基线时为淀粉样蛋白阳性的 MCI 患者中有 9 名转化为痴呆,均为 AD 型。11 名淀粉样蛋白阴性的 MCI 患者中有 3 名转化为痴呆,但均未转化为 AD 所致痴呆。PPV、NPV 和准确率(痴呆:0.53、0.73 和 0.61;AD:0.53、1.00 和 0.70)与神经心理学测试相当,优于 ApoE 基因分型。
所有转化为 AD 所致痴呆的 MCI 患者均为淀粉样蛋白阳性。然而,只有 50%的 AD 型 MCI 患者在 24 个月后出现明显的 AD 所致痴呆,限制了[(11)C]PiB PET 对临床结局的个体预测的实用性。